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Effects of Liothyronine In The Prevention of Electroshock-Induced Cognitive Side Effects

Effects of Liothyronine In The Prevention of ECT-Induced Cognitive Side Effects

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015081823673N1
Enrollment
66
Registered
2015-09-14
Start date
2015-04-05
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Condition 1: bipolar disorder. Condition 2: depressive disorder. Bipolar affective disorder depressive episode

Interventions

Intervention 1: intervention group: liothyronine tab 1 microgram per kilogram once daily in the morning and oral from 1 day before first ECT session to 1 month after last ECT session. Intervention 2:
Treatment - Drugs
Placebo
intervention group: liothyronine tab 1 microgram per kilogram once daily in the morning and oral from 1 day before first ECT session to 1 month after last ECT session.
control group: placebo tab with the same shape and size of liothyrone tablet,once daily in the morning and oral, from 1 day before first ECT session to 1 month after last ECT session.

Sponsors

Kashan University of Medical Science Vise Chancellor for Research
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: inclusion criteria: men and women 18 to 45 years old with mood disorder diagnosis(major depressive disorder or bipolar disorder)based on DSM4TR criteria; candidate of ECT; without sensitivity to liothyronine; negative pregnancy test before treatment initiation; using safe contraception during the study. exclusion criteria: unstable cardiovascular disease; history of myocardial infarction in past 3 months; current unstable angina; untreated endocrine disorders; uncontrolled hypertention; structural brain anomaly; cerebral infarct or hemorrhage in past 1 month; unstable or bleeding vascular anneurism; severe respiratory disorders that are contraindications of general anesthesia; decompensating heart problems; heart vulvular disorders; brain space occupying lesions leading to increased intracranial pressure; pregnancy; addiction( except smoking) during the study; ECT treatment in past 6 months; allergic reaction to liothyronine; mental retardation; delirium, dementia or other amnestic disorders; occurrence of ECT-induced delirium during the study; lithium administration during the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Memory. Timepoint: before first ECT session, before 4th ECT session, 1 month after last ECT session. Method of measurement: wechsler memory scale.

Secondary

MeasureTime frame
Altered thyroid function. Timepoint: before 4th ECT session and 1 month after last ECT session. Method of measurement: thyroid function blood test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactPooya Hazegh

Kashan University of Medical Science Vice Chancellor for Research

pooyahazegh@gmail.com+98 31 5554 9111

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026